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Padmavati Pharmaceuticals

FDA import alert and refusal historyHaridwar, IndiaFEI 3010880044

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Example subjectPadmavati Pharmaceutical added to Import Alert 16-129 (red list)

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As of October 25, 2026, Padmavati Pharmaceuticals (Haridwar, India) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for deltas pancha tulasi drops basils - 5, published by FDA on June 22, 2017, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Padmavati Pharmaceuticals

1 record, newest first. Each line links to the FDA page it came from.

2017

  1. Import alert listing
    Listed on Import Alert 99-39red listDeltas Pancha Tulasi Drops Basils - 5
    Source

Questions about Padmavati Pharmaceuticals

Is Padmavati Pharmaceuticals on an FDA import alert?
Yes. As of October 25, 2026, Padmavati Pharmaceuticals is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for deltas pancha tulasi drops basils - 5; FDA published the listing on June 22, 2017.
Has FDA refused shipments from Padmavati Pharmaceuticals?
No FDA import refusals for Padmavati Pharmaceuticals appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Padmavati Pharmaceuticals's FEI number?
Padmavati Pharmaceuticals's FDA Establishment Identifier (FEI) is 3010880044.
Can shipments from Padmavati Pharmaceuticals still enter the U.S.?
Shipments of deltas pancha tulasi drops basils - 5 from Padmavati Pharmaceuticals can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectPadmavati Pharmaceutical added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.